The Journal of Organic Chemistry · 2019 · 20 citations · 36 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistryOrganometallic ChemistrySynthetic Medicinal ChemistryCross-coupling ReactionsHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsMacrocycle SynthesisAromatic Ring ExpansionFused Heterocycle SynthesisHeteroaromatic CompoundsHeterocycle DiversificationHeterocyclic Ring Expansion
-bromosuccinimide mediation are described. We have expanded the scope of this ring expansion methodology and investigated the effect substituents on the aromatic ring, and the cyclobutanol moiety, have on the outcome of the reaction. Limitations with certain substituents on the cyclobutanol moiety are also described. Further experimental evidence to support our mechanistic understanding is disclosed, and we now preclude the suggested involvement of a primary radical for this transformation.
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Vincent W. Bowry, Janusz Lusztyk, K. U. Ingold · Journal of the American Chemical Society · 1991 · 242 citations